EP0289003A2 - Méthode immunologique et réactif pour la détermination d'un antigène polyvalent dans un échantillon liquide - Google Patents
Méthode immunologique et réactif pour la détermination d'un antigène polyvalent dans un échantillon liquideInfo
- Publication number
- EP0289003A2 EP0289003A2 EP88106763A EP88106763A EP0289003A2 EP 0289003 A2 EP0289003 A2 EP 0289003A2 EP 88106763 A EP88106763 A EP 88106763A EP 88106763 A EP88106763 A EP 88106763A EP 0289003 A2 EP0289003 A2 EP 0289003A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- antibody
- receptor
- antigen
- bindable
- fragments
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Images
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
- G01N33/54366—Apparatus specially adapted for solid-phase testing
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/74—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving hormones or other non-cytokine intercellular protein regulatory factors such as growth factors, including receptors to hormones and growth factors
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/824—Immunological separation techniques
Definitions
- the invention relates to an immunochemical method and reagent for determining a polyvalent, ie. H. at least bifunctional antigen in a liquid sample.
- polyvalent antigens peptides, proteins
- B The sensitive determination of polyvalent antigens (peptides, proteins) using two antibodies directed against different antigen determinants is known, e.g. B. from J. Clin. Chem. Clin. Biochem. 18 (1980) 197-208. Numerous variants of this method have become known, for example from DE-OS 34 00 027. According to this OS, an incubation with three different receptors is carried out to determine the polyvalent antigen, of which the first and the third are present in solution in the liquid phase and with the Antigen are capable of binding, while the second receptor is in the solid phase and is capable of binding to the first receptor and the third receptor is labeled and does not cross-react with the first and second receptors.
- a disadvantage of the methods and reagents based on this principle lies in the unsatisfactory stability of the reagents used for this.
- the stability of the calibration curve is shown here under stability (Signal / concentration of the analyte) understood over a longer period of time.
- the unsatisfactory stability has the consequence that the calibration curves of the freshly prepared reagents do not match the calibration curves of the stored reagent. As a rule, one observes that the calibration curve becomes flatter with increasing storage. The reasons for this are not known.
- the object of the invention is now to improve a method and a reagent of the type described above so that the stability of the calibration curve is given over a longer period of time than before, in other words, the reliability of double antibody sandwich methods (DASP) is improved.
- DASP double antibody sandwich methods
- this object is achieved by a method for the quantitative determination of a polyvalent antigen by incubation with three different receptors, of which the first (R1) and the third (R3) are dissolved in the liquid phase and are capable of binding to the antigen, the second receptor ( R2) is in the solid phase and is bindable with (R1) and (R3) has a label and does not cross-react with (R1) and (R2), separation of the solid from the liquid phase and measurement of the label in one of the phases, which is thereby characterized in that a first receptor (R1) is used, which consists of at least two interconnected antibody molecules or antibody molecule fragments, at least one of which specifically binds to the antigen to be determined.
- the receptors used in the context of the invention are specifically bindable substances, in particular either specific bindable complete antibodies, which can be polyclonal or monoclonal, their antibody fragments or conjugates of antibodies or antibody fragments with haptens or antigens. Monoclonal antibodies are preferably used.
- antibody or “antibody molecule” means not only the complete antibodies but also their bindable fragments, which are known to the person skilled in the art.
- a polyvalent antigen is understood here as an antigen with several antigenic determinants.
- the two receptors R1 and R2 form a substance pair that is specifically bindable to one another.
- the receptor R2 can be an immunoglobulin or protein A directed against the receptor R1 if the receptor R1 is an antibody.
- the receptor R2 can be avidin, streptavidin or biotin if the receptor R1 is a biotinylated or provided with avidin antibody.
- Other substance pairs are suitable and known to the person skilled in the art.
- the first receptor (R1) preferably consists of identical antibodies crosslinked with one another or bindable fragments thereof, which can be monoclonal or polyclonal.
- the individual antibody molecules are connected to each other by bivalent or polyvalent linkers (bridge-building).
- Crosslinking by means of divalent linkers is preferred, since they enable easier control of the "degree of polymerization" of the receptor.
- the effect according to the invention is also achieved with polyvalent linkers.
- linkers Compounds which have reactive groups which are capable of reacting in aqueous solution with the functional groups of proteins to form a covalent formation can be used as linkers (bridging agents).
- linkers bridging agents
- a large number of suitable bifunctional or polyfunctional linkers are known to the person skilled in the art.
- Typical examples of homo- or heterobifunctional and trifunctional linkers which are very suitable in the context of the invention are listed in Table 1 below.
- a solution of the antibodies to be connected to one another can be mixed with the linker molecules under conditions which lead directly to the crosslinking.
- the degree of crosslinking in this case is controlled by the amount of linker added.
- the crosslinking is preferably carried out in such a way that one half of the antibodies to be connected to one another is reacted with a first linker under conditions in which only one of the functions of the linker leads to formation with the antibody.
- the other half of the antibodies to be crosslinked is reacted in an analogous manner with a second linker.
- the two antibody derivatives thus obtained are then reacted with one another.
- a molar ratio of the to one another is preferred
- Antibody derivatives to be connected between 2: 1 and 1: 2 applied. A ratio of about 1: 1 is particularly preferred.
- the receptor (R1) preferably contains 2 to 20 antibody molecules, particularly preferably 4 to 12 antibody molecules.
- the receptor (R1) can also be composed of two different antibodies which are directed towards the antigen to be determined and towards the Receptor (R2) each have a well-specific binding ability.
- the complete receptor (R1) is produced by the preferred method of individual derivatization of the two different antibodies described above and subsequent reaction of the two derivatives with one another.
- a receptor R1 is preferred which has a composition which is as uniform as possible with regard to its degree of polymerization or the number of individual antibody molecules contained therein. This can be achieved in a simple manner by pre-purification by chromatography.
- a receptor which is bound to an insoluble phase and which is capable of binding to the receptor (R1) is used as the receptor (R2).
- R2 is preferably an antibody in the sense of the above definition.
- (R2) is either with a part of the receptor (R1) composed of homologous antibodies is bindable or, in the case of a heterogeneously composed receptor (R1), bindable to the component which has the lower affinity for the antigen to be determined.
- the receptor (R2) is preferably directed against the Fc part of an antibody molecule in the receptor (R1).
- a receptor (R2) which is generally directed against the Fc part of immunoglobulin is also suitable.
- the third receptor (R3) is capable of binding to the polyvalent antigen to be determined. It can contain a polyclonal or monoclonal antibody. If it is a monoclonal antibody, it is chosen so that it binds to another epitope such as (R1). This can be achieved in a simple manner by using a monoclonal antibody which is capable of binding to the polyvalent antigen to be determined both in (R1) and in (R3), these monoclonal antibodies recognizing different antigenic determinants. This has the advantage that both antibodies can come from the same test animal.
- the receptor R3 also carries a label.
- the label can be an enzyme, a radioactive substance, an isotope, a fluorescent or chemiluminescent substance, the determination of which is carried out according to one of the methods well known to the person skilled in the art.
- an enzyme such as peroxidase or ⁇ -galactosidase
- the activity of this enzyme can be measured in the manner generally known for this purpose by using a known detection reagent for this labeling enzyme, e.g. B. a color reagent, adds and measures either in the presence of the solid phase or after separation. The enzyme activity measured is then a measure of the amount of polyvalent antigen to be determined.
- Another object of the invention is a reagent for the quantitative determination of a polyvalent antigen containing 3 receptors (R1, R2, R3), of which (R1) and (R3) are soluble and capable of binding to the antigen, (R3) is labeled and with ( R1) and (R2) do not cross-react, which is characterized in that (R1) consists of at least two interconnected antibody molecules or antibody molecule fragments, at least one of which binds specifically to the antigen to be determined.
- the invention improves the stability of the reagents for heterogeneous immunoassays, such as the double antibody sandwich method, in particular with regard to the constancy of the calibration curve over a longer period of time.
- the improved constancy of the calibration curve improves the reliability of the determination.
- a rotor insert element for automatic centrifugal analyzers consisting of a molded body which has at least one mixing valve chamber and a measuring chamber, which have a sample application chamber, which is connected to a plurality of reagent fields, each of which contains an absorbent carrier material impregnated with a specific reagent, and a measuring chamber, which together has a sample liquid transport path form, which leads from radially inside to radially outside when the insert element is fastened on the rotor and further at least one further chamber for receiving a liquid and a transport path leading from this chamber to the measurement guide and which is at least partially identical to the sample liquid transport path, having.
- the sample liquid transport path leads from a sample application chamber (P) a chamber (a) containing buffer, filled with absorbent material, a chamber (c) and a first valve chamber (Vk1) arranged between the chambers (a) and (c) to a second valve chamber (Vk2) and from there via the chamber ( d) and via a collecting chamber (AK) to the measuring chamber (K).
- a substrate chamber (PK) designed as a pump chamber is provided to hold another liquid and is connected to the second valve chamber (Vk2) via a metering device consisting of a metering chamber (DK) and a capillary (Kap) and an overflow chamber (ÜK).
- Fig. 1 shows schematically the rotor insert element used.
- Reagent carrier 1 or 1 ' is placed on field c of the rotor insert element and reagent carrier 2 on field d.
- 40 ⁇ l of a sample diluted 1: 3 with 0.9% NaCl solution are pipetted directly into the field a through an opening at the upper edge.
- 270 ⁇ l of substrate solution are pipetted into chamber PK.
- a suitable centrifugation program in which high speeds alternate with standstill, the sample and substrate solution are then conveyed in the direction of the separation matrix and cuvette.
- the receptors (R3) and (R1) or (R1 ′) are eluted from the field c by the sample liquid and the homogeneous mixture is then reacted.
- the complexes formed are bound to the receptor (R2).
- the sample is transferred from field c to d in a very short time.
- the substrate solution is divided into portions by the dosing chamber DK, the first of which are used to wash out excess, non-complexed conjugate.
- the ⁇ -galactosidase activity bound to d via complex formation is proportional to that contained in the sample AFP amount or at the sample blank value. This activity is determined with a further portion of the substrate, the substrate being converted into colored products in a five-minute reaction. The color formed and the further color development / min in the liquid phase are measured in the cuvette at 576 nm.
- FIGS. 2 and 3 show the results when using 400 ng / AK / test in the reagent carrier 1 ′ and 1.
- Table II shows the results for 400 and 800 ng AK / test.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Molecular Biology (AREA)
- Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- General Health & Medical Sciences (AREA)
- Pathology (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Physics & Mathematics (AREA)
- Cell Biology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Endocrinology (AREA)
- Peptides Or Proteins (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19873714147 DE3714147A1 (de) | 1987-04-28 | 1987-04-28 | Immunchemisches verfahren und reagenz zur bestimmung eines polyvalenten antigens in einer fluessigen probe |
DE3714147 | 1987-04-28 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0289003A2 true EP0289003A2 (fr) | 1988-11-02 |
EP0289003A3 EP0289003A3 (fr) | 1991-04-10 |
EP0289003B1 EP0289003B1 (fr) | 1994-06-29 |
Family
ID=6326435
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP88106763A Expired - Lifetime EP0289003B1 (fr) | 1987-04-28 | 1988-04-27 | Méthode immunologique et réactif pour la détermination d'un antigène polyvalent dans un échantillon liquide |
Country Status (7)
Country | Link |
---|---|
US (1) | US4885255A (fr) |
EP (1) | EP0289003B1 (fr) |
JP (1) | JPH0731203B2 (fr) |
KR (1) | KR900008958B1 (fr) |
AT (1) | ATE108023T1 (fr) |
DE (2) | DE3714147A1 (fr) |
ES (1) | ES2056074T3 (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0809111A2 (fr) * | 1996-05-24 | 1997-11-26 | Roche Diagnostics GmbH | Procede d'analyse utilisant des recepteurs oligomeres |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3922960A1 (de) * | 1989-07-12 | 1991-01-17 | Boehringer Mannheim Gmbh | Verfahren zur bestimmung eines analyten |
US5648218A (en) * | 1993-02-12 | 1997-07-15 | Sealite Sciences, Inc. | Preparation of photoprotein conjugates and methods of use thereof |
DE69430523T2 (de) * | 1993-02-12 | 2002-11-28 | Sealite Sciences, Inc. | Herstellung von photoprotein konjugaten und verfahren zu ihrer verwendung |
US5556759A (en) * | 1993-08-02 | 1996-09-17 | Beach; Peter G. | Assay and method for determining newborn risk for sudden infant death syndrome |
US20040018577A1 (en) | 2002-07-29 | 2004-01-29 | Emerson Campbell John Lewis | Multiple hybrid immunoassay |
US9233382B2 (en) * | 2006-07-27 | 2016-01-12 | Ossian, Inc. | Liquid spraying apparatus |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0074271A1 (fr) * | 1981-09-08 | 1983-03-16 | Ortho Diagnostic Systems Inc. | Liaison de deux anticorps |
EP0105714A1 (fr) * | 1982-09-29 | 1984-04-18 | Serono Diagnostics Limited | Immunoessai pour antigènes |
EP0147848A2 (fr) * | 1984-01-02 | 1985-07-10 | Roche Diagnostics GmbH | Méthode pour la détermination d'un antigèn polyvalent et réactif |
EP0205198A1 (fr) * | 1985-04-29 | 1986-12-17 | Stichting Vrienden Van De Stichting Dr. Karl Landsteiner | Complexe immunologique, sa préparation et son utilisation |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE337223B (fr) * | 1967-05-23 | 1971-08-02 | Pharmacia Ab | |
US4376110A (en) * | 1980-08-04 | 1983-03-08 | Hybritech, Incorporated | Immunometric assays using monoclonal antibodies |
DE3225027A1 (de) * | 1982-07-05 | 1984-01-05 | Boehringer Mannheim Gmbh, 6800 Mannheim | Immunchemisches messverfahren |
US4659678A (en) * | 1982-09-29 | 1987-04-21 | Serono Diagnostics Limited | Immunoassay of antigens |
DE3345748A1 (de) * | 1983-12-17 | 1985-08-29 | Boehringer Mannheim Gmbh, 6800 Mannheim | Phenolsulfonphthaleinyl-ss-d-galactoside, verfahren zu deren herstellung sowie deren verwendung zur bestimmung der ss-d-galactosidase |
DE3400027A1 (de) * | 1984-01-02 | 1985-07-18 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren zur bestimmung eines polyvalenten antigens und reagenz hierfuer |
DE3425008A1 (de) * | 1984-07-06 | 1986-02-06 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren und vorrichtung zur durchfuehrung analytischer bestimmungen |
US4657853A (en) * | 1984-09-14 | 1987-04-14 | E. I. Du Pont De Nemours And Company | Immunoassays utilizing covalent conjugates of polymerized enzyme and antibody |
JPH0656383B2 (ja) * | 1985-02-22 | 1994-07-27 | オリンパス光学工業株式会社 | 酵素免疫学的自動分析装置 |
-
1987
- 1987-04-28 DE DE19873714147 patent/DE3714147A1/de not_active Withdrawn
-
1988
- 1988-03-28 US US07/173,779 patent/US4885255A/en not_active Expired - Lifetime
- 1988-04-25 JP JP63100445A patent/JPH0731203B2/ja not_active Expired - Lifetime
- 1988-04-27 AT AT88106763T patent/ATE108023T1/de not_active IP Right Cessation
- 1988-04-27 DE DE3850439T patent/DE3850439D1/de not_active Expired - Lifetime
- 1988-04-27 EP EP88106763A patent/EP0289003B1/fr not_active Expired - Lifetime
- 1988-04-27 ES ES88106763T patent/ES2056074T3/es not_active Expired - Lifetime
- 1988-04-28 KR KR1019880004839A patent/KR900008958B1/ko not_active IP Right Cessation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0074271A1 (fr) * | 1981-09-08 | 1983-03-16 | Ortho Diagnostic Systems Inc. | Liaison de deux anticorps |
EP0105714A1 (fr) * | 1982-09-29 | 1984-04-18 | Serono Diagnostics Limited | Immunoessai pour antigènes |
EP0147848A2 (fr) * | 1984-01-02 | 1985-07-10 | Roche Diagnostics GmbH | Méthode pour la détermination d'un antigèn polyvalent et réactif |
EP0205198A1 (fr) * | 1985-04-29 | 1986-12-17 | Stichting Vrienden Van De Stichting Dr. Karl Landsteiner | Complexe immunologique, sa préparation et son utilisation |
Non-Patent Citations (1)
Title |
---|
Biochemical Journal vol. 173, 1978, Great Britain Seiten 723 - 737; J. Carlsson et al.: "Protein thiolation and reversible protein-protein conjugation. N-succinimidyl 3-[2-pyridyldithioÜpropionate, a new heterobifunctional reagent " * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0809111A2 (fr) * | 1996-05-24 | 1997-11-26 | Roche Diagnostics GmbH | Procede d'analyse utilisant des recepteurs oligomeres |
EP0809111A3 (fr) * | 1996-05-24 | 1999-01-07 | Roche Diagnostics GmbH | Procede d'analyse utilisant des recepteurs oligomeres |
Also Published As
Publication number | Publication date |
---|---|
US4885255A (en) | 1989-12-05 |
DE3850439D1 (de) | 1994-08-04 |
KR900008958B1 (ko) | 1990-12-15 |
KR880013013A (ko) | 1988-11-29 |
JPS63284470A (ja) | 1988-11-21 |
EP0289003A3 (fr) | 1991-04-10 |
EP0289003B1 (fr) | 1994-06-29 |
ATE108023T1 (de) | 1994-07-15 |
ES2056074T3 (es) | 1994-10-01 |
JPH0731203B2 (ja) | 1995-04-10 |
DE3714147A1 (de) | 1988-11-17 |
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